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HRID 29743作成日:2026年10月27日

Diisopropylethylamine → 2-[(1-Benzyloxycarbonylamino-2-methylpropyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl ester

https://huagongshe.com/reaction/29743

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物PyBOPHCID 2724699—
反応物(1-Benzyloxycarbonylamino-2-methyl-propyl)-phosphonic acid monomethyl esterHCID 10380108—
反応物5-Tert-butoxycarbonylamino-2-hydroxy-pentanoic acid methyl esterHCID 54330025—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2-[(1-Benzyloxycarbonylamino-2-methylpropyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl esterHCID 5439201869%

反応手順

A solution of PyBOP (2.1 g, 4.0 mmol) in DMF (3 mL) was added to a mixture of (1-benzyloxycarbonylamino-2-methyl-propyl)-phosphonic acid monomethyl ester (1.0 g, 3.32 mmol) and 5-tert-butoxycarbonylamino-2-hydroxy-pentanoic acid methyl ester (865 mg, 3.5 mmol) in DMF (4 mL) under argon. DIPEA (2.28 mL, 13.3 mmol) was added dropwise and the mixture was stirred over night. Ethyl acetate was added and the mixture was washed with 10% KHSO4, satd. NaHCO3 and brine and dried. Concentration under reduced pressure followed by chromathography (heptane/EtOAc, 1:1→1:6) gave 2-[(1-benzyloxycarbonylamino-2-methyl-propyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl ester (1.21 g, 69%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423012B2
出典データセットuspto-grants-2008_09
ORD IDord-b6f4d112812d4f00b22a247b00911401
出典メモuspto-grants-2008_09